AdvGeneMap2018Commands
From Statistical Genetics Courses
Plink Data QC
#PLINK plink --file GWAS plink --file GWAS --mind 0.10 --recode --out GWAS_clean_mind plink --file GWAS_clean_mind --maf 0.05 --recode --out MAF_greater_5 plink --file GWAS_clean_mind --exclude MAF_greater_5.map --recode --out MAF_less_5 plink --file MAF_greater_5 --geno 0.05 --recode --out MAF_greater_5_clean plink --file MAF_less_5 --geno 0.01 --recode --out MAF_less_5_clean plink --file MAF_greater_5_clean --merge MAF_less_5_clean.ped MAF_less_5_clean.map --recode --out GWAS_MAF_clean plink --file GWAS_MAF_clean --mind 0.03 --recode --out GWAS_clean2 plink --file GWAS_clean2 --check-sex --out GWAS_sex_checking #### in R - open R by simply typing R setwd("to_your_working_directory/") sexcheck = read.table("GWAS_sex_checking.sexcheck", header=T) names(sexcheck) sex_problem = sexcheck[which(sexcheck$STATUS=="PROBLEM"),] sex_problem q() ################################## plink --file GWAS_clean2 --genome --out duplicates #### in R setwd("to_your_working_directory/") dups = read.table("duplicates.genome", header = T) problem_pairs = dups[which(dups$PI_HAT > 0.4),] problem_pairs problem_pairs = dups[which(dups$PI_HAT > 0.05),] myvars = c("FID1", "IID1", "FID2", "IID2", "PI_HAT") problem_pairs[myvars] q() ###### plink --file GWAS_clean2 --remove IBS_excluded.txt --recode --out GWAS_clean3 plink --file GWAS_clean3 --het ###### in R Dataset <- read.table("plink.het", header=TRUE, sep="", na.strings="NA", dec=".", strip.white=TRUE) mean(Dataset$F) sd(Dataset$F) jpeg("hist.jpeg", height=1000, width=1000) hist(scale(Dataset$F), xlim=c(-4,4)) dev.off() q() ###### plink --file GWAS_clean3 --pheno pheno.txt --pheno-name Aff --hardy ##### in R hardy = read.table("plink.hwe", header = T) names(hardy) hwe_prob = hardy[which(hardy$P < 0.0000009),] hwe_prob q() ########## plink --file GWAS_clean3 --exclude HWE_out.txt --recode --out GWAS_clean4